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/ Immunexpress, Inc.
Immunexpress, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K232095
SeptiCyte RAPID
December 15, 2023
K203748
SeptiCyte RAPID
November 29, 2021
K163260
SeptiCyte LAB
February 17, 2017